← Back to catalogue

Venus Versa

FDA UDI

Class II (US FDA UDI)

by Venus Concept Inc.

Identity

Trade Name
Venus Versa FDA UDI
Generic Name
Multi-modality skin surface treatment system generator FDA UDI
Device Name
The Venus Versa system is a multi-application device intended to be used in aesthetic and cosmetic procedures. FDA UDI
Model / Reference
VE102407 FDA UDI
Description
The Venus Versa system is a multi-application device intended to be used in aesthetic and cosmetic procedures. FDA UDI

Identifiers

Primary DI / UDI-DI
07290016540383 FDA UDI
FDA Product Code
ONF FDA UDI
GEI FDA UDI
GMDN Term
Multi-modality skin surface treatment system generator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-modality skin surface treatment system generator

Venus Versa by Venus Concept Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin surface treatment system generator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Venus Concept Inc.

Sources (1)

  • FDA UDI cb38785a-6a59-4461-8c0b-6822c2c6380c 33 fields · synced May 30, 2026